510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K893462Substantially Equivalent

Nu-Trap Suction Catheter W/mucus Trap

Atheus Corp., Los Angeles CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893462 is the FDA 510(k) clearance record for NU-TRAP SUCTION CATHETER W/MUCUS TRAP, a class I device, cleared for Atheus Corp. on under FDA product code BSY (Catheters, Suction, Tracheobronchial). FDA records list 2 510(k) clearances for Atheus Corp., from to . As of , FDA records show no recalls naming K893462.

Clearance record

Decision date
Received
(36 days to decision)
Product code
BSY Catheters, Suction, Tracheobronchial
Regulation
21 CFR 868.6810
Device class
Class I
Review panel
Anesthesiology
Applicant
Atheus Corp. Suite 1200 Two Century Plz., Los Angeles CA
Third party review
No

Clearances, product code BSY

Trailing 12 months

FDA records hold no clearances under product code BSY in the trailing twelve months.

FDA records show no clearances under product code BSY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BSY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260